Trietsch Sebastiaan J, Naumovska Elena, Kurek Dorota, Setyawati Meily C, Vormann Marianne K, Wilschut Karlijn J, Lanz Henriëtte L, Nicolas Arnaud, Ng Chee Ping, Joore Jos, Kustermann Stefan, Roth Adrian, Hankemeier Thomas, Moisan Annie, Vulto Paul
Mimetas BV, JH Oortweg 19, 2333CH, Leiden, The Netherlands.
Roche Innovation Center Basel, F. Hoffmann-La Roche Ltd, Grenzacherstrasse 124, 4070, Basel, Switzerland.
Nat Commun. 2017 Aug 15;8(1):262. doi: 10.1038/s41467-017-00259-3.
In vitro models that better reflect in vivo epithelial barrier (patho-)physiology are urgently required to predict adverse drug effects. Here we introduce extracellular matrix-supported intestinal tubules in perfused microfluidic devices, exhibiting tissue polarization and transporter expression. Forty leak-tight tubules are cultured in parallel on a single plate and their response to pharmacological stimuli is recorded over 125 h using automated imaging techniques. A study comprising 357 gut tubes is performed, of which 93% are leak tight before exposure. EC-time curves could be extracted that provide insight into both concentration and exposure time response. Full compatibility with standard equipment and user-friendly operation make this Organ-on-a-Chip platform readily applicable in routine laboratories.Efforts to determine the effects of drugs on epithelial barriers could benefit from better in vitro models. Here the authors develop a microfluidic device supporting the growth and function of extracellular matrix-supported intestinal tubules, and evaluate the effect of staurosporine and acetylsalicylic acid on barrier integrity.
迫切需要能更好反映体内上皮屏障(病理)生理学的体外模型来预测药物不良反应。在此,我们介绍了灌注微流控装置中由细胞外基质支撑的肠小管,其呈现出组织极化和转运体表达。在单个平板上并行培养40个无渗漏的小管,并使用自动成像技术在125小时内记录它们对药理刺激的反应。进行了一项包含357个肠管的研究,其中93%在暴露前无渗漏。可以提取出能洞察浓度和暴露时间反应的EC-时间曲线。与标准设备完全兼容且操作方便,使得这个芯片器官平台易于在常规实验室中应用。确定药物对上皮屏障影响的研究可以从更好的体外模型中受益。在此,作者开发了一种支持细胞外基质支撑的肠小管生长和功能的微流控装置,并评估了星形孢菌素和乙酰水杨酸对屏障完整性的影响。